Webinar · Palm Beach, Florida
How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters
Hospital · Medical Equipment · Education, Training
Key numbers
- Editions on record
- 1first in 2011
About How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters
This GCP compliance in Clinical Trials training aims to provide an overview of the parameters critical in ensuring GCP compliance and in doing this, will translate GCP in a more practical, applied sense.
Applying GCP in a real life situation is often subjective, requires experience and training. A Clinical Trial, like any other project is divided in stages with tasks running in parallel or in sequence and affecting one another in a cause and effect relationship. Over the years, findings of inspectors and experiences of monitors have identified clusters of deficiencies in complying with GCP principles, key areas that emanate straight from the GCP guidelines.
Areas Covered in the Seminar:
- Importance of Good Clinical Practice.
- Key areas of deficiencies in Clinical trials.
- Common findings in audits and inspections.
- Definition of ranking of findings: minor-major-critical.
- Definition of Adverse and Serious adverse events.
- ICH guidelines on the Informed consent process.
- Management of investigational drug.
- Investigator site file and essential documents.
- Source data.
- Site and people management.
From our listing of this edition. Details may have changed since.
Editions
| Year | Dates | Where | Exhibitors | Visitors |
|---|---|---|---|---|
| 2011 | 4 Oct 2011 | Webinar Venue Online | — | — |
Past editions from the bvents archive (2008–2019) and organiser figures where they were published.
Questions
When is How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters?
The next dates haven't been confirmed. The last edition we have on record was 4 Oct 2011.
Where is it held?
The last edition we have was at Webinar Venue, Palm Beach, Florida.